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rs1057522024

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522024(A;G)
Make rs1057522024(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41144518
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1057522024
dbSNP (old)rs1057522024
ClinGenrs1057522024
ebirs1057522024
HLIrs1057522024
Exacrs1057522024
Gnomadrs1057522024
Varsomers1057522024
Maprs1057522024
PheGenIrs1057522024
Biobankrs1057522024
1000 genomesrs1057522024
hgdprs1057522024
ensemblrs1057522024
gopubmedrs1057522024
geneviewrs1057522024
scholarrs1057522024
googlers1057522024
pharmgkbrs1057522024
gwascentralrs1057522024
openSNPrs1057522024
23andMers1057522024
23andMe allrs1057522024
SNPshotrs1057522024
SNPdbers1057522024
MSV3drs1057522024
GWAS Ctlgrs1057522024
Max Magnitude0
ClinVar
Risk rs1057522024(G;G)
Alt rs1057522024(G;G)
Reference Rs1057522024(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41003771A>G
CLNSRC
CLNACC RCV000430135.1,